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Ulta beauty ear care - Medication Information

Product NDC Code 70094-009
Drug Name

Ulta beauty ear care

Type Brand
Active Ingredients
Benzalkonium chloride 1.2 mg/ml
Route TOPICAL
Dosage Form SOLUTION
RxCUI drug identifier 1052949
Application Number M003
Labeler Name The Richline Group, Inc.
Packages
Package NDC Code Description
70094-009-01 118 ml in 1 bottle (70094-009-01)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient Benzalkonium Chloride 0.12% w/w Purpose Antiseptic

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
Directions For optimal results, follow these steps daily: Clean hands thoroughly with soap before touching ears or piercing studs. Using a cotton swab saturated with Ear Care solution, cleanse front and back of piercing 3 time daily. Gently rotate the earrings while cleasnsing. DO NOT remove earrings. Keep hair, hair spray, shampoo, soap, cosmetics, perfume, etc. away from newly pierced ears. After shampooing, exercising, swimming, or use of hair products, rinse ears in clear water and reapply Ear Care Solution.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients Purified Water

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
Use First aid to prevent infection of pierced ears.

Purpose

Information about the drug product’s indications for use.
Purpose Antiseptic

Spl product data elements

Usually a list of ingredients in a drug product.
Ulta Beauty Ear Care BENZALKONIUM CHLORIDE WATER BENZALKONIUM CHLORIDE BENZALKONIUM

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
Package Labeling: Label1

Spl unclassified section

Information not classified as belonging to one of the other fields. Approximately 40% of labeling with effective_time between June 2009 and August 2014 have information in this field.
Drug Facts

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
Keep out of reach of children.

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
Questions? Call 1-800-255-8556

Stop use

Information about when use of the drug product should be discontinued immediately and a doctor consulted. Includes information about any signs of toxicity or other reactions that would necessitate immediately discontinuing use of the product.
Stop use and ask a doctor if you experience pain, redness, or swelling.

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
Warnings For external use only. Do not ingest. If swallowed, get medical help or contact Poison Control Center immediately. In case of contact with eyes, flush with water. Keep out of reach of children. Stop use and ask a doctor if you experience pain, redness, or swelling.

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API